Variant #0000017958 (NC_000009.11:g.35657914G>A, NR_003051.3:n.102C>T (RMRP))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.35657914G>A
DNA change (hg38) g.35657917G>A
Published as 101C>T
ISCN -
DB-ID RMRP_000102 See all 2 reported entries
Variant remarks 1 Belgian CHH patient (com-het); Variants n.91G>A and n.101C>T are in same haplotype and it is unclear which of them is (or both are) causative
Reference PubMed: Hermanns el al. 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2013-04-22 14:21:13 +02:00 (CEST)
Date last edited 2020-06-25 13:27:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RMRP NR_003051.3 +?/+? - n.102C>T r.102c>u -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.